NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2107667 Query DataSets for GSM2107667
Status Public on Sep 26, 2016
Title ETV6-RUNX1-22
Sample type RNA
 
Source name bone marrow
Organism Homo sapiens
Characteristics diagnosis: b-cell precursor acute lymphoblastic leukemia (BCP-ALL)
Extracted molecule total RNA
Extraction protocol Total RNA was harvested with the miRNeasy mini kit (Qiagen) with Dnase treatment on-column.
Label Cy3
Label protocol Cyanine-3 (Cy3) labeled cRNA was prepared from 100 ng RNA using the One-Color Low Input Quick Amp Labling kit (Agilent) according to the manufacturer's instructions, followed by miRNeasy column purification (Qiagen). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
 
Hybridization protocol 600 ng of Cy3-labelled cRNA (specific activity >6 pmol Cy3/ug cRNA) was fragmented at 60°C for 30 minutes in a reaction volume of 25µl containing 1x Agilent fragmentation buffer and 2x Agilent blocking agent following the manufacturers instructions. On completion of the fragmentation reaction, 25 µl of 2x GEx Hybridization buffer HI-RPM was added to the fragmentation mixture and hybridized to the array for 17 hours at 65°C in a rotating hybridization oven. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent).
Scan protocol Slides were scanned immediately after washing on the Agilent DNA Microarray Scanner with SureScan High-Resolution Technology using one color scan setting for 8x60k array slides (Scan Area 61x21.6 mm, Scan resolution 3µm, Dye channel is set to Green).
Description Gene expression of T-ALL patient blood sample
Data processing The scanned images were analyzed with Feature Extraction Software (Agilent) using default parameters (protocol GE1-105_Dec08 and Grid: 041648_D_F_20120615) to obtain background subtracted and spatially detrended Processed Signal intensities.
 
Submission date Apr 04, 2016
Last update date Sep 26, 2016
Contact name Farzaneh Ghazavi
E-mail(s) farzaneh.ghazavi@ugent.be
Organization name Gent university hospital
Department Center of medical genetics
Street address De Pintelaan 185
City Ghent
ZIP/Postal code 9000
Country Belgium
 
Platform ID GPL19197
Series (2)
GSE79869 Lnc-RNA expression pattern in ETV6/RUNX1-driven b-cell precursor acute lymphoblastic leukemia (BCP-ALL)
GSE79873 Unique long non-coding RNA expression signature in ETV6/RUNX1-driven B-cell precursor acute lymphoblastic leukemia

Data table header descriptions
ID_REF
VALUE Normalized signal intensity.

Data table
ID_REF VALUE
A_33_P3400429 6.868178018
A_33_P3255531 3.569338105
A_24_P940149 6.710579937
A_33_P3306510 11.47107932
CUST_21085_PI427704219 3.706469942
A_33_P3348313 7.848489009
A_33_P3403361 10.23134463
A_33_P3348973 7.388902548
A_23_P11070 6.673402256
A_24_P274615 8.444501451
CUST_1480_PI427704219 3.832114328
CUST_13414_PI427704219 4.420832245
A_24_P928969 1.988118094
A_23_P100074 8.536750097
A_33_P3227506 4.899171583
CUST_17237_PI427704219 9.130819016
CUST_12234_PI427704219 1.799273887
A_32_P47643 6.495497473
CUST_802_PI427704219 2.606849348
A_33_P3542886 4.249473775

Total number of rows: 43357

Table truncated, full table size 1190 Kbytes.




Supplementary file Size Download File type/resource
GSM2107667_ETV6-RUNX1-22.txt.gz 3.1 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap